Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis Diagnosis

This work’s goal was to research new candidate antigens for cutaneous leishmaniosis (CL). In order to reach the goal, we used random peptide phage display libraries screened using antibodies from Leishmania braziliensis patients. After selection, three peptides (P1, P2, and P3) were synthesized usin...

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Main Authors: Juliana Seger Link, Silvana Maria Alban, Carlos Ricardo Soccol, Gilberto Vinicius Melo Pereira, Vanete Thomaz Soccol
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2017/5871043
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author Juliana Seger Link
Silvana Maria Alban
Carlos Ricardo Soccol
Gilberto Vinicius Melo Pereira
Vanete Thomaz Soccol
author_facet Juliana Seger Link
Silvana Maria Alban
Carlos Ricardo Soccol
Gilberto Vinicius Melo Pereira
Vanete Thomaz Soccol
author_sort Juliana Seger Link
collection DOAJ
description This work’s goal was to research new candidate antigens for cutaneous leishmaniosis (CL). In order to reach the goal, we used random peptide phage display libraries screened using antibodies from Leishmania braziliensis patients. After selection, three peptides (P1, P2, and P3) were synthesized using Fmoc chemistry. The peptides individually or a mixture of them (MIX) was subsequently emulsified in complete and incomplete Freund’s adjuvant and injected subcutaneously in golden hamsters. Sera from the hamsters administered with P1 presented antibodies that recognized proteins between 76 and 150 kDa from L. braziliensis. Sera from hamsters which had peptides P2 and P3, as well as the MIX, administered presented antibodies that recognized proteins between 52 and 76 kDa of L. braziliensis. The research on the similarity of the peptides’ sequences in protein databases showed that they match a 63 kDa glycoprotein. The three peptides and the MIX were recognized by the sera from CL patients by immunoassay approach (ELISA). The peptides’ MIX showed the best performance (79% sensitivity) followed by the P1 (72% sensitivity), and the AS presented 91% sensitivity. These results show a new route for discovering molecules for diagnosis or for immunoprotection against leishmaniosis.
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institution Kabale University
issn 2314-8861
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language English
publishDate 2017-01-01
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series Journal of Immunology Research
spelling doaj-art-59d745b3d0a2410f8ba8759a76c3beff2025-02-03T01:32:56ZengWileyJournal of Immunology Research2314-88612314-71562017-01-01201710.1155/2017/58710435871043Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis DiagnosisJuliana Seger Link0Silvana Maria Alban1Carlos Ricardo Soccol2Gilberto Vinicius Melo Pereira3Vanete Thomaz Soccol4Basic Pathology Department, Federal University of Paraná, Curitiba, PR, BrazilDepartment of Bioprocess Engineering and Biotechnology, Federal University of Paraná, Curitiba, PR, BrazilDepartment of Bioprocess Engineering and Biotechnology, Federal University of Paraná, Curitiba, PR, BrazilDepartment of Bioprocess Engineering and Biotechnology, Federal University of Paraná, Curitiba, PR, BrazilBasic Pathology Department, Federal University of Paraná, Curitiba, PR, BrazilThis work’s goal was to research new candidate antigens for cutaneous leishmaniosis (CL). In order to reach the goal, we used random peptide phage display libraries screened using antibodies from Leishmania braziliensis patients. After selection, three peptides (P1, P2, and P3) were synthesized using Fmoc chemistry. The peptides individually or a mixture of them (MIX) was subsequently emulsified in complete and incomplete Freund’s adjuvant and injected subcutaneously in golden hamsters. Sera from the hamsters administered with P1 presented antibodies that recognized proteins between 76 and 150 kDa from L. braziliensis. Sera from hamsters which had peptides P2 and P3, as well as the MIX, administered presented antibodies that recognized proteins between 52 and 76 kDa of L. braziliensis. The research on the similarity of the peptides’ sequences in protein databases showed that they match a 63 kDa glycoprotein. The three peptides and the MIX were recognized by the sera from CL patients by immunoassay approach (ELISA). The peptides’ MIX showed the best performance (79% sensitivity) followed by the P1 (72% sensitivity), and the AS presented 91% sensitivity. These results show a new route for discovering molecules for diagnosis or for immunoprotection against leishmaniosis.http://dx.doi.org/10.1155/2017/5871043
spellingShingle Juliana Seger Link
Silvana Maria Alban
Carlos Ricardo Soccol
Gilberto Vinicius Melo Pereira
Vanete Thomaz Soccol
Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis Diagnosis
Journal of Immunology Research
title Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis Diagnosis
title_full Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis Diagnosis
title_fullStr Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis Diagnosis
title_full_unstemmed Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis Diagnosis
title_short Synthetic Peptides as Potential Antigens for Cutaneous Leishmaniosis Diagnosis
title_sort synthetic peptides as potential antigens for cutaneous leishmaniosis diagnosis
url http://dx.doi.org/10.1155/2017/5871043
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AT silvanamariaalban syntheticpeptidesaspotentialantigensforcutaneousleishmaniosisdiagnosis
AT carlosricardosoccol syntheticpeptidesaspotentialantigensforcutaneousleishmaniosisdiagnosis
AT gilbertoviniciusmelopereira syntheticpeptidesaspotentialantigensforcutaneousleishmaniosisdiagnosis
AT vanetethomazsoccol syntheticpeptidesaspotentialantigensforcutaneousleishmaniosisdiagnosis